Detecting Overall Survival Benefit Derived From Survival Postprogression Rather Than Progression-Free Survival

被引:18
|
作者
Morita, Satoshi [1 ]
Sakamaki, Kentaro [2 ]
Yin, Guosheng [3 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Biomed Stat & Bioinformat, Kyoto 6068507, Japan
[2] Yokohama City Univ, Dept Biostat & Epidemiol, Grad Sch Med, Yokohama, Kanagawa 232, Japan
[3] Univ Hong Kong, Dept Stat & Actuarial Sci, Hong Kong, Hong Kong, Peoples R China
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2015年 / 107卷 / 08期
关键词
METASTATIC BREAST-CANCER; SURROGATE END-POINT; DISEASE-CONTROL; OPEN-LABEL; EFFICACY; ERIBULIN; TIME;
D O I
10.1093/jnci/djv133
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Broglio and Berry (2009) examined the impact of survival postprogression (SPP) on overall survival (OS) when progression-free survival (PFS) was used to assess treatment effect in metastatic cancer. Their simulation studies found no statistical difference in OS because of dilution effect from SPP, although there was a statistical difference in PFS between treatment arms. Recently, two phase III clinical trials showed efficacy of experimental treatments in OS, but not PFS. These results seem counterintuitive, because it may be reasonable to consider that the effect of treatment in prolonging PFS can influence OS prolongation. We conducted simulations to examine the role of SPP in OS under the assumption that only SPP, and not PFS, differed between treatment arms. We also explored the impact of patient heterogeneity on the OS analysis. Our study offers a reasonable explanation for the two phase III trials and recommends further discussion of PFS as an adequate endpoint and what role SPP might play in OS to evaluate current treatment regimens.
引用
收藏
页数:4
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